Canonical Allele Identifier: CA2662705635
Gene: BMPR2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.202519074_202519075del , CM000664.2:g.202519074_202519075del GRCh38
NC_000002.11:g.203383797_203383798del , CM000664.1:g.203383797_203383798del GRCh37
NC_000002.10:g.203092042_203092043del NCBI36
NG_009363.1:g.147748_147749del , LRG_712:g.147748_147749del

Transcript Alleles

HGVS Amino-acid Change
ENST00000374580.10:c.852+22_852+23del MANE Select ENSP00000363708.4:n.852+22_852+23del
ENST00000638587.1:c.783+22_783+23del ENSP00000491062.1:n.783+22_783+23del
ENST00000374574.2:c.852+22_852+23del ENSP00000363702.2:n.852+22_852+23del
ENST00000374580.8:c.852+22_852+23del ENSP00000363708.4:n.852+22_852+23del
NM_001204.6:c.852+22_852+23del , LRG_712t1:c.852+22_852+23del NP_001195.2:n.852+22_852+23del
XM_011511687.1:c.852+22_852+23del XP_011509989.1:n.852+22_852+23del
XM_011511688.1:c.852+22_852+23del XP_011509990.1:n.852+22_852+23del
NM_001204.7:c.852+22_852+23del MANE Select NP_001195.2:n.852+22_852+23del